Overexpression of Lewis y antigen promotes human epididymis protein 4-mediated invasion and metastasis of ovarian cancer cells

Biochimie ◽  
2014 ◽  
Vol 105 ◽  
pp. 91-98 ◽  
Author(s):  
Huiyu Zhuang ◽  
Zhenhua Hu ◽  
Mingzi Tan ◽  
Liancheng Zhu ◽  
Juanjuan Liu ◽  
...  
2014 ◽  
Vol 13 (1) ◽  
pp. 243 ◽  
Author(s):  
Huiyu Zhuang ◽  
Mingzi Tan ◽  
Juanjuan Liu ◽  
Zhenhua Hu ◽  
Dawo Liu ◽  
...  

2004 ◽  
Vol 92 (3) ◽  
pp. 896-904 ◽  
Author(s):  
Nicholas B Berry ◽  
Yong Mee Cho ◽  
Maureen A Harrington ◽  
Stephen D Williams ◽  
John Foley ◽  
...  

2014 ◽  
Vol 2 (4) ◽  
pp. 247-259

Semaphorins are a large family of genes involved in the development and morphogenesis of the nervous system. SEMA5A has been reported as a bi-functional molecule, acting as both oncogene and tumor suppressor in different types of cancer. High expression levels of SEMA5A and its receptor, Plexin-B3, were associated with aggressiveness in pancreatic and prostate cancers. Our previous study in ovarian cancer metastasis indicates that FAK knock-down can suppress ovarian cancer cells migration and invasion. We hypothesized that SEMA5A expression promotes ovarian cancer invasion and metastasis. We investigated the expression of SEMA5A in patients with metastatic ovarian cancer (n = 43), localized tumor (n = 37) and normal ovarian tissue (n = 12) from non-malignant diseases as control with different histopathological characteristics. For Silencing of SEMA5A in vitro, we treated human ovarian cancer cells (OVCAR-3, A2780/CP70) with miR-27a and miR-27b. We observed significantly higher expression of SEMA5A protein (P= 0.001) in metastatic ovarian cancer tissue associated with poor overall survival outcomes compared to localized ovarian cancer and control. In vitro silencing of SEMA5A reduced migration and invasion of ovarian cancer cell. Our data offer opportunities for the therapeutic modulation and biomarker of metastatic ovarian cancer.


PLoS ONE ◽  
2013 ◽  
Vol 8 (7) ◽  
pp. e68994 ◽  
Author(s):  
Huiyu Zhuang ◽  
Jian Gao ◽  
Zhenhua Hu ◽  
Juanjuan Liu ◽  
Dawo Liu ◽  
...  

2020 ◽  
Vol 9 (5) ◽  
pp. 3691-3702
Author(s):  
Haifeng Qiao ◽  
Jinwei Liu ◽  
Zhixia Yang ◽  
Leilei Gao ◽  
Xiaolan Zhang ◽  
...  

2016 ◽  
Vol 26 (6) ◽  
pp. 994-1003 ◽  
Author(s):  
Ying-Chun Wang ◽  
Yi-Nan Wu ◽  
Su-Li Wang ◽  
Qing-Hua Lin ◽  
Ming-Fang He ◽  
...  

ObjectiveWe investigated the effect of docosahexaenoic acid (DHA) on the invasion and metastasis of ovarian cancer cells (A2780, HO8910, and SKOV-3).MethodsCytotoxicity assay was performed to determine the optimal doses of DHA in this experiment. The effects of DHA on invasion ability were assessed by invasion assay. The expressions of messenger RNA and/or proteins associated with invasion or metastasis were detected by quantitative Real Time-Polymerase Chain Reaction or Western blot. The effect of DHA on cell metastasis was assessed in xenograft model of zebrafish.ResultsDocosahexaenoic acid and α-linolenic acid could reduce the cell vitalities in dose-dependent manner. However, DHA inhibited the invasion and metastasis of ovarian cancer cells, but α-linolenic acid did not (**P < 0.01). Docosahexaenoic acid could downregulate the expressions of WAVE3, vascular endothelial cell growth factor, and MMP-9, and upregulate KISS-1, TIMP-1, and PPAR-γ, which negatively correlated with cell invasion and metastasis (*P < 0.05). Docosahexaenoic acid restrained the development of subintestinal vessels and cancer cell metastasis in xenograft model of zebrafish (**P < 0.01).ConclusionsDocosahexaenoic acid inhibited the invasion and metastasis of ovarian cancer cells in vitro and in vivo through the modulation of NF-κB signaling pathway, suggesting that DHA is a promising candidate for ovarian cancer therapy.


Sign in / Sign up

Export Citation Format

Share Document